Reported Apr 23, 2025 · Ongoing

Medline Convenience kits used for various procedures

MEDLINE INDUSTRIES, LP - Northfield

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: MEDLINE INDUSTRIES, LP - Northfield · 3 Lakes Dr · Northfield, IL · 60093-2753

Is this the product you have?

Medline Convenience kits used for various procedures

33 of 33 products

Products covered by this recall
Model / numberProduct as published
DYNJ43914BOCULOPLASTIC PICK PACK
DYNJ65109PLASTIC PACK
DYNJ34160DPLASTIC PROCEDURE PACK
DYNJ84991MINOR BREAST SJHC-LF
DYNJ66056PLASTIC PACK
DYNJ66212AMUSCLE PLASTIC PACK
DYNJ37231BMINOR PLASTIC PACK
DYNJ52658DGENERAL BREAST GRH-LF
DYNJ52658DGENERAL BREAST GRH-LF
DYNJ37316DFACE PACK
DYNJ57440DPLASTIC PACK-LF
DYNJ84991MINOR BREAST SJHC-LF
DYNJ37231BMINOR PLASTIC PACK
DYNJ63696SATELLITE MINOR PLASTIC PACK
DYNJ68328FACIAL/EYE PACK
DYNJ63753BREAST PACK
DYNJ63753BREAST PACK
DYNJ64886ATUMMY PACK
DYNJ46737APLASTIC TORSO PK TEGH-LF
DYNJ40620FPLASTIC BREAST PACK
Lot codes and dates

33 of 33 products

Products covered by this recall
#BarcodesProduct as published
11019348924382640193489243827Lot Number: 24IBH633; 2) DYNJ65109, UDI-DI: 10193489243826(each), 40193489243827(case)
21088994221354240889942213543Lot Number: 24IBH739; 3) DYNJ34160D, UDI-DI: 10889942213542(each), 40889942213543(case)
31019532744407540195327444076Lot Number: 24IBH802; 4) DYNJ84991, UDI-DI: 10195327444075(each), 40195327444076(case)
41019348931812840193489318129Lot Number: 24IBL195; 5) DYNJ66056, UDI-DI: 10193489318128(each), 40193489318129(case)
51019532734507540195327345076Lot Number: 24IBR304; 6) DYNJ66212A, UDI-DI: 10195327345075(each), 40195327345076(case)
61088438987165240884389871653Lot Number: 24JBL025; 7) DYNJ37231B, UDI-DI: 10884389871652(each), 40884389871653(case)
71019532746882840195327468829Lot Number: 24JBM075; 8) DYNJ52658D, UDI-DI: 10195327468828(each), 40195327468829(case)
81019532746882840195327468829Lot Number: 24JBM318; 9) DYNJ52658D, UDI-DI: 10195327468828(each), 40195327468829(case)
91019348967276340193489672764Lot Number: 24JBM914; 10) DYNJ37316D, UDI-DI: 10193489672763(each), 40193489672764(case)
101019348923865540193489238656Lot Number: 24JBT528; 11) DYNJ57440D, UDI-DI: 10193489238655(each), 40193489238656(case)
111019532744407540195327444076Lot Number: 24JBT877; 12) DYNJ84991, UDI-DI: 10195327444075(each), 40195327444076(case)
121088438987165240884389871653Lot Number: 24JBV138; 13) DYNJ37231B, UDI-DI: 10884389871652(each), 40884389871653(case)
131019348975470440193489754705Lot Number: 24JBV645; 14) DYNJ63696, UDI-DI: 10193489754704(each), 40193489754705(case)
141019348982355440193489823555Lot Number: 24JBV846; 15) DYNJ68328, UDI-DI: 10193489823554(each), 40193489823555(case)
151019348975733040193489757331Lot Number: 24JBW152; 16) DYNJ63753, UDI-DI: 10193489757330(each), 40193489757331(case)
161019348975733040193489757331Lot Number: 24JBW480; 17) DYNJ63753, UDI-DI: 10193489757330(each), 40193489757331(case)
171019348991635540193489916356Lot Number: 24JBX780; 18) DYNJ64886A, UDI-DI: 10193489916355(each), 40193489916356(case)
181088994211655340889942116554Lot Number: 24JBX789; 19) DYNJ46737A, UDI-DI: 10889942116553(each), 40889942116554(case)
191019532763132140195327631322Lot Number: 24KBA440; 20) DYNJ40620F, UDI-DI: 10195327631321(each), 40195327631322(case)
201019845916603740198459166038Lot Number: 24KBB123; 21) DYNJ64712B, UDI-DI: 10198459166037(each), 40198459166038(case)
Amount recalled
4094 units

This recall covers 34 products

The agency filed one notice per product. You are reading one of them; the other 33 are below.

21 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:35 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.